HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403670Generated: October 30, 2026
Sodium Carbonate → 2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-3-carboxylic acid
https://huagongshe.com/reaction/1403670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Carboxyphenylboronic acid | HCID 2733957 | — |
| Reactant | {1-[2-Bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamic acid tert-butyl ester | HCID 67407943 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethoxyethane ethanol water | HCID 86587095 | — |
| Product | 2'-(1-tert-Butoxycarbonylamino-ethyl)-5'-(3-fluoro-pyridin-4-ylcarbamoyl)-biphenyl-3-carboxylic acid | HCID 67409767 | — |
Reaction Steps
To a solution of {1-[2-bromo-4-(3-fluoro-pyridin-4-ylcarbamoyl)-phenyl]-ethyl}-carbamicacid tert-butyl ester (2841 μmol) and 3-carboxyphenylboronic acid (1.5 eq.) in a mixture of DME/EtOH/water: 1/1/1 (10 ml) was added Na2CO3 (4 eq) and Pd tetrakis (0.05 eq). The reaction mixture was heated in the microwave at 130° C. for 1.5 hours. The reaction mixture was diluted with water and citric acid (to acidic pH) and extracted with EtOAc. The combined organic layers were dried over MgSO4 and the solvent was removed under reduced pressure. The compound was purified by column chromatography (silicagel, DCM/MeOH gradient).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912209B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-fda90fd4ed6545158ee75d226cf37f77 |
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| Source note | uspto-grants-2014_12 |
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